Kdm2a inhibition in skeletal muscle improves metabolic flexibility in obesity

Skeletal muscle is a critical organ in maintaining homoeostasis against metabolic stress, and histone post-translational modifications are pivotal in those processes. However, the intricate nature of histone methylation in skeletal muscle and its impact on metabolic homoeostasis have yet to be elucidated. Here, we report that mitochondria-rich slow-twitch myofibers are characterized by significantly higher levels of H3K36me2 along with repressed expression of Kdm2a, an enzyme that specifically catalyses H3K36me2 demethylation. Deletion or inhibition of Kdm2a shifts fuel use from glucose under cold challenge to lipids under obese conditions by increasing the proportion of mitochondria-rich slow-twitch myofibers. This protects mice against cold insults and high-fat-diet-induced obesity and insulin resistance. Mechanistically, Kdm2a deficiency leads to a marked increase in H3K36me2 levels, which then promotes the recruitment of Mrg15 to the Esrrg locus to process its precursor messenger RNA splicing, thereby reshaping skeletal muscle metabolic profiles to induce slow-twitch myofiber transition. Collectively, our data support the role of Kdm2a as a viable target against metabolic stress.

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Publication Details

Journal
Nature Metabolism
Published
2025-01-27
DOI
https://doi.org/10.1038/s42255-024-01210-9
Citations
15
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
17.46

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article

Kdm2a inhibition in skeletal muscle improves metabolic flexibility in obesity

Teng Huang, Danni Song, Cong‐Yi Wang, Zhichao Gao et al.
15 citations
Nature Metabolism
Adipose Tissue and Metabolism
17.46
article

Kdm2a inhibition in skeletal muscle improves metabolic flexibility in obesity

Teng Huang, Danni Song, Cong‐Yi Wang, Zhichao Gao, Hao Yin, Ruihan Dong, Hao Xie, Jinghan Zhu, Qianrui Liu, Fei Sun, Jia Gao, Xin Liu, Yi Wang, Shiwei Liu, Ting Wang, Shu Zhang, Na Wang, Qilin Yu, Wen Kong, Xi Luo, Yang Li, Yuhan Wang
article en
15 citations

Abstract

Skeletal muscle is a critical organ in maintaining homoeostasis against metabolic stress, and histone post-translational modifications are pivotal in those processes. However, the intricate nature of histone methylation in skeletal muscle and its impact on metabolic homoeostasis have yet to be elucidated. Here, we report that mitochondria-rich slow-twitch myofibers are characterized by significantly higher levels of H3K36me2 along with repressed expression of Kdm2a, an enzyme that specifically catalyses H3K36me2 demethylation. Deletion or inhibition of Kdm2a shifts fuel use from glucose under cold challenge to lipids under obese conditions by increasing the proportion of mitochondria-rich slow-twitch myofibers. This protects mice against cold insults and high-fat-diet-induced obesity and insulin resistance. Mechanistically, Kdm2a deficiency leads to a marked increase in H3K36me2 levels, which then promotes the recruitment of Mrg15 to the Esrrg locus to process its precursor messenger RNA splicing, thereby reshaping skeletal muscle metabolic profiles to induce slow-twitch myofiber transition. Collectively, our data support the role of Kdm2a as a viable target against metabolic stress.

Nature MetabolismVol. 7(2)
Union Hospital (HK), Shanxi Medical University (CN), Second Military Medical University (CN), Wuhan University (CN), Shanghai Changzheng Hospital (CN), Changhai Hospital (CN), Wuhan Union Hospital (CN), Renmin Hospital of Wuhan University (CN), Shanxi Academy of Medical Sciences (CN), Tongji Hospital (CN), Union Hospital (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 1%
Adipose Tissue and Metabolism
17.46
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